pain relief
- Product NDC
- 79481-3000
- 11-digit product format
- 794813000
- Labeler code
- 79481
- Product ID
- 79481-3000_84529dbd-730e-440b-bd0c-c42499c91823
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Meijer, Inc.
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 2024-02-07
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| WK2XYI10QM | IBUPROFEN | 15687-27-1 | IBUPROFEN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 79481-3000-0 | 79481300000 | 250 TABLET, FILM COATED in 1 BOTTLE (79481-3000-0) | 2024-02-07 | No | No | Historical |